| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:149939064-149939300 | Rare:48 | ||||
| chr1:149950026-149950250 | Common:4; Rare:67 | ||||
| chr1:149950540-149950577 | Common:1; Rare:8 | ||||
| chr1:150009675-150009749 | Common:1; Rare:12 | ||||
| chr1:150009765-150009894 | Rare:18 | ||||
| chr1:150061692-150061976 | Common:2; Rare:40 | ||||
| chr1:150065626-150065761 | Common:1; Rare:11 | ||||
| chr1:150109722-150109823 | Common:2; Rare:18 | ||||
| chr1:150110178-150110620 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:150111212-150111436 | Common:3; Rare:36 | ||||
| chr1:150163023-150163569 | Common:5; Rare:126 | ||||
| chr1:150213577-150213867 | Common:2; Rare:70 | ||||
| chr1:150213968-150214022 | Rare:9 | ||||
| chr1:150235314-150235335 | Rare:4 | ||||
| chr1:150236855-150236978 | Rare:12 |